A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028574



Internal ID18771105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:327447..412579hg38UCSC Ensembl
Innerchr5:327562..412694hg19UCSC Ensembl
Innerchr5:380562..465694hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3885133
hg1985133
hg1885133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633215
Samples
Known GenesAHRR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028574
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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